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Chapter 8
ENVIRONMENTAL
HEALTH
&
TOXICOLOGY
2
OUTLINE
• ENVIRONMENTAL HEALTH
 INFECTIOUS AND EMERGENT DISEASES
 ANTIBIOTICS AND PESTICIDE RESISTANCE
• TOXICOLOGY
• MOVEMENT, DISTRIBUTION, AND FATE OF
TOXINS
• MINIMIZING TOXIC EFFECTS
• MEASURING TOXICITY
• RISK ASSESSMENT
• ESTABLISHING HEALTH POLICY
3
ENVIRONMENTAL HEALTH
• HEALTH - a state of complete physical, mental,
and social well-being
• DISEASE - an abnormal change in the body’s
condition that impairs physical or
psychological function, disrupting
HOMEOSTASIS
 Diet and nutrition, infectious agents, toxic
chemicals, genetics, trauma and
psychological stress all play roles in
MORBIDITY (illness) and MORTALITY (death).
4
ENVIRONMENTAL HEALTH RISKS
5
ENVIRONMENTAL HEALTH RISKS
• PATHOGENS - INFECTIOUS AGENTS – bacteria,
fungus, virus, parasite, protozoa, etc
• TRAUMA – accidents
• POLLUTION – air, water, noise, etc
• RADIATION – UV, nuclear waste
• TOXINS – smoking, metals like mercury & lead,
chemical exposure from pesticides, herbicides,
cleaning solution, etc.
6
Categories of Human Health Risk
• The categories of health risk:
 PHYSICAL – cause injury or loss of life (natural
disaster, UV radiation, rock thrown at your
head)
 BIOLOGICAL – involved diseases (causes
most deaths)
 CHEMICAL – exposure to natural or synthetic
chemicals (pesticides, pharmaceuticals, heavy
metals)
7
Categories of Human Health Risk
• Types of diseases
 INFECTIOUS DISEASES are caused by
pathogens, which include viruses, bacteria,
fungi, protests, worms (transmitted by
contact…COMMUNICABLE)
 CHRONIC DISEASES slowly impair the
functioning of a body (long lasting and
recurrent) (heart disease, cancer)
 ACUTE DISEASES rapidly impair bodily
functions (flu, stroke)
• Chronic much higher in developing countries due
to poor sanitation, unsafe water, malnutrition, etc
8
GLOBAL DISEASE BURDEN
• Life expectancy is increasing as infant mortality
decreases.
• Disability-adjusted life years (DALYs) – a tool
that measures the effects of a disease on the
population. DALY’s takes into account ALL
effects of a disease. Not just the number of
people who die from it.
• Chronic conditions account for 60% of
premature deaths and 50% of diseases and are
becoming more prevalent.
 By 2020, heart disease may become leading
source of disability and disease worldwide.
Global cancer rates will increase by 50%.
9
GLOBAL DISEASE BURDEN
• DIABETES is on the increase. One-third of
children born in North America today will
develop diabetes in their lifetime due to poor
diet and little exercise.
• WHO projects that PSYCHOLOGICAL
CONDITIONS could increase their share of the
global disease burden from 10% currently to
15%.
 DEPRESSION will be the second largest
cause of all years lived with disability.
• TOBACCO RELATED LUNG DISEASES are
increasing. Biggest single cause of death
worldwide.
10
CAUSES
OF
GLOBAL
DISEASE
BURDEN
11
COMMON VECTORS & DISEASES
• VECTOR – the mode of transport for a pathogenic
organism
• INSECTS:
 MOSQUITOES (malaria, dengue, yellow fever)
 FLIES (sleeping sickness, typhoid, cholera)
 TICKS (Lyme, Rocky Mt Spotted Fever)
• WATER BORNE DISEASES:
diarrheas, Hepatitis A, typhoid, cholera
• VIRUSES: Hepatitis, HIV, measles, small pox
• PROTOZOANS: malaria, giardia, trypanosomiasis
• WORMS: tapeworm, flukes, schistosomiasis,
elephantatiasis
• RODENTS, BIRDS, etc. can also carry pathogens
12
INFECTIOUS DISEASES KILL PEOPLE
• When a pathogen causes a rapid increase
in disease, we call it an EPIDEMIC
• When it occurs over a large geographic
area, we call it a PANDEMIC
• Transferred through spit/sneezing,
contaminated foods/objects, vectors
• Antibiotics are over prescribed and
pathogens becoming resistant making
“stronger” bacteria
13
INFECTIOUS DISEASES
• Communicable diseases are still responsible for
about 1/3 of all disease-related deaths.
- Majority in countries with poor nutrition,
sanitation, and vaccination
 Malaria is a major disease in tropical
areas. Two million people die each year.
• Better nutrition, clean water, improved sanitation
and inoculation of children could eliminate most
of the deaths.
14
HISTORICAL DISEASES
• PLAGUE caused by bacteria carried by fleas
• MALARIA is caused by protists found in
mosquitoes
• TUBERCULOSIS is a highly contagious disease
caused by bacteria that attacks the lungs
• FLU - Greatest loss of life in a single year from
a pathogen was in 1918 when the flu epidemic
killed 50 to 100 million people worldwide.
Today we are concerned that bird flu might
cause an even larger outbreak.
15
EMERGENT DISEASES
• An EMERGENT DISEASE is one never known
before, or one which has been absent for at
least 20 years.
• Growing human populations push into remote
areas where they encounter pathogens.
• Air travel makes it possible to spread emergent
diseases around the globe quickly.
 West Nile virus (spread by mosquitoes) was
introduced into North America in 1999, and is
now found everywhere in the lower 48 states.
16
EMERGENT INFECTIOUS DISEASES
• HIV - HUMAN IMMUNODEFICIENCY SYNDROME /
Acquired Immune Deficiency Syndrome (AIDS) –
came from chimps. Weakens immune system
• EBOLA comes from primates. Fever, internal
bleeding. No pandemic, but death within two
weeks
• MAD COW DISEASE – pathogen that damages
cow’s nervous system. Can have same affect on
humans (attack brain)
• BIRD FLU – Small number infects now, but future
worse
• WEST NILE spread by mosquitoes
• SARS (severe acute respiratory syndrome)
17
RECENT OUTBREAKS
18
CONSERVATION MEDICINE
• ECOLOGICAL DISEASES - ANIMAL EPIDEMICS
 A viral hemorrhagic disease is killing fish in
the Great Lakes; introduced through ballast.
 California sea lions have herpes 1 virus
spread to them from human sewage.
 Mad Cow and Deer wasting Disease are
spread by prions from animal to animal
 Sudden oak death syndrome is killing oak,
redwoods, Douglas fir trees. Fungus
imported on nursery stock.
19
CONSERVATION MEDICINE
• CONSERVATION MEDICINE - attempts to
understand how environmental changes
threaten the health of humans and natural
communities
• ZOONOTIC ILLNESS – diseases normally found
in animals that can be spread to humans
(Anthrax, Rabies, Lyme, Plague, West Nile,
Tuberculosis, Brucellosis)
20
ANTIBIOTIC AND PESTICIDE RESISTANCE
• WHAT CAUSES RESISTANCE?
 Natural selection and the ability of organisms
to evolve rapidly
 Human tendency to overuse pesticides and
antibiotics
• IE: Protozoan parasite that causes malaria is
now resistant to most antibiotics, while the
mosquitoes that transmit it have developed
resistance to many insecticides. And, Global
Warming is widening the range of these insects.
21
ANTIBIOTIC USE
• At least half of the 100 million antibiotic doses
prescribed in the U.S. every year are
unnecessary or are the wrong drug.
• Many people do not finish the full-course.
Allowing resistant bacteria to multiply.
• More than half of all antibiotics manufactured in
the U.S. are routinely fed to farm animals to
stimulate weight gain. Excreted in urine and
feces, they find their way into surface water.
22
ANTIBIOTIC RESISTANCE
23
FUNDING HEALTH CARE
• Heaviest burden of illness borne by poorest
people who cannot afford a healthy
environment or adequate health care.
 WHO estimates 90% of all disease burden
occurs in developing countries where less
than 10% of all health care dollars are spent.
• Raising our investment in health care would
boost the world economy, reduce the spread of
pathogens, and reduce population growth since
parents whose children survive have fewer
offspring.
24
25
TOXICOLOGY
• TOXICOLOGY is the study of poisons and their
effects on living systems.
• Dangerous chemicals are divided into two
broad categories:
 TOXIC - poisonous
- Can be general or very specific. Often
harmful even in dilute concentrations.
 HAZARDOUS - dangerous
- Flammable, explosive, irritant, acid, caustic
• ECOTOXICOLOGY deals with the interactions,
transformation, fate, and effects of natural and
synthetic chemicals in the biosphere.
26
REMEMBER: The level of harmfulness depends
on dose, frequency, genetic make up of those
exposed, and health of those exposed
TOXICOLOGY
CHEMICALS OF CONCERN 7 CATEGORIES
1. IMMUNE SYSTEM DEPRESSANTS - pollutants
that depress the immune system
2. ENDOCRINE DISRUPTERS - disrupt normal
hormone functions (DDT, plastics)
 cause low sperm count, breast cancer
 Environmental estrogens - environmental
contaminants which cause reproductive
problems in animals even at very low doses
27
3. NEUROTOXINS - metabolic poisons that
specifically attack nerve cells, cause organ
failure (insecticides, lead, mercury).
Different types act in different ways.
 HEAVY METALS kill nerve cells.
 ANESTHETICS AND CHLORINATED
HYDROCARBONS disrupt nerve cell
membranes.
 ORGANOPHOSPHATES AND CARBAMATES
inhibit signal transmission between nerve
cells.
28
4. MUTAGENS - Agents that damage or alter
genetic material. Can lead to birth defects or
tumors. (chloroform, ethylene oxide, benzene,
lead, and vinyl chloride)
5. TERATOGENS - specifically cause
abnormalities during embryonic growth and
development
(nicotine, alcohol, drugs)
 Alcohol - Fetal Alcohol Syndrome
6. CARCINOGENS - chemicals that cause cancer.
Cause cell damage and causes bad cells to
grow. Damage genetic material (radon, arsenic,
PCB’s, asbestos)
29
ABNORMAL CELL GROWTH aka Tumors
• Many carcinogens, teratogens, and mutagens
are dangerous at levels far below their direct
toxic effect because abnormal cell growth
exerts a form of biological amplification. One
cell mutated by a toxin can form a tumor that
can potentially kill an individual.
Remember... cells grow exponentially!
BENIGN – a tumor that grows slowly and doesn’t
interfere with normal cell functions
MALIGNANT - a growth that grows rapidly and
interferes with normal cell functions
30
7. ALLERGENS - substances that causes high
response from immune system (mold, pollen,
dander, peanuts)
 ANTIGENS - substances that are recognized as
foreign by white blood cells and stimulate the
production of specific antibodies
- Other allergens act indirectly by binding to
other materials so they become antigenic.
 SICK BUILDING SYNDROME (SBS) is a
phenomenon affecting building occupants
who claim to experience acute health and
comfort effects that appear to be linked to time
spent in a building, but where no specific
illness or cause can be identified.
31
MOVEMENT,
DISTRIBUTION,
AND FATE OF
TOXINS
32
MOVEMENT, DISTRIBUTION, AND FATE OF TOXINS
33
MOVEMENT, DISTRIBUTION, AND FATE OF
TOXINS
• SOLUBILITY - one of most important
characteristics in determining the movement and
storage of a toxin
• Chemicals are divided into two major groups:
 WATER SOLUBLE (dissolve in water)
compounds move rapidly through the
environment and have access to cells.
 FAT SOLUBLE (dissolve in oil) compounds
need a carrier to move through the
environment, but once inside the body they
penetrate tissues easily. They are stored in
body fat and persist for many years.
34
EXPOSURE AND SUSCEPTIBILITY
• Airborne toxins generally cause more ill health
than any other exposure.
 Lining of lungs easily absorbs toxins.
• Food, water and skin contact are other ways to
be exposed to toxins.
• Largest toxin exposure reported in industrial
settings
• Condition of organism and timing of exposure
also have strong influences on toxicity.
Children more vulnerable than adults.
• BODY BURDEN - accumulated toxins in the
body
35
• BIOACCUMULATION
selective absorption &
storage of toxins
 Dilute toxins in the
environment can build to
dangerous levels inside
tissues.
• BIOMAGNIFICATION
Toxic burden of a large
number of organisms at a
lower trophic level is
accumulated and
concentrated by a predator
at a higher trophic level.
36
PERSISTENCE
• Some chemical compounds are very unstable
and degrade rapidly under most conditions,
thus their concentrations decline quickly after
release.
• Others are more persistent.
 Stability can cause problems as toxins may
be stored for a long period of time and
spread to unintended victims
PERSISTENCE- how long a chemical remains in
the environment
37
38
PERSISTENT ORGANIC POLLUTANTS - POP’s
• FLAME RETARDANTS (PBDE) are now found in
humans and other species everywhere in the
world. Harm children’s reproductive and
nervous systems.
• NON-STICK PLASTIC COATINGS (PFOS and
PFOA) are infinitely persistent in the
environment and can be found in your blood.
Cause liver damage and cancer.
• PHTHALATES - found in plastics mimic
estrogen and are linked to reproductive
abnormalities and reduced fertility.
39
CHEMICAL INTERACTIONS
• ANTAGONISTIC REACTION - one material
interferes with the effects, or stimulates the
breakdown, of other chemicals
• ADDITIVE REACTION - effects of each chemical
are added to one another
• SYNERGISTIC REACTION - one substance
exacerbates the effect of the other
 Example: Asbestos exposure increases risk
of lung cancer 20X; smoking has same risk.
But together, they increase risk 400X.
40
MECHANISMS FOR MINIMIZING TOXIC EFFECTS
• EVERY MATERIAL CAN BE POISONOUS
UNDER CERTAIN CONDITIONS.
 Most chemicals have a safe threshold under
which their effects are insignificant.
• METABOLIC DEGRADATION
 In mammals, the LIVER is the primary site of
detoxification of both natural and introduced
poisons.
- Sometimes compounds that are harmless
can be broken down into products that are
harmful.
41
EXCRETION AND REPAIR
• Effects of waste products and environmental
toxins reduced by eliminating via excretion.
 Breathing
 Urine
• Tissues and organs often have mechanisms for
damage repair by cellular reproduction.
 Any irritating agent can be potentially
carcinogenic because the more times that
cells divide, the greater the chance that they
will have a mistake (mutation) while copying
their DNA. This can lead to cancer.
42
DOSE-RESPONSE STUDIES
• EPIDEMIOLOGY - gathers data from large
exposed populations over long periods and
compares with a population group not exposed
the threat
• DOSE-RESPONSE ANALYSIS measures
response of test animals to various doses of
suspected toxicant
 DOSE = the amount of toxicant the test animal
receives
 RESPONSE = the type or magnitude of
negative effects of the animal
 DOSE-RESPONSE CURVE = the plot of dose
given against response
43
DOSE-RESPONSE STUDIES
• LD50- “median Lethal Dose” that kills 50% of the
individuals in 2 weeks
• ED50- “median Effective Dose” that causes 50%
of the animals to display the harmful but
nonlethal effect
• LC50 – “median Lethal Concentration” that kills
50% of aquatic species
• Not very accurate as different animals & people
respond differently.
• Helps us determine at what levels of pollution,
drugs, and other substances we should/should
not be exposed.
44
45
46
47
Most members in this population are similar,
however there are extremes at both ends
48
0-10 very sensitive
10-30 relatively sensitive (20 is average)
30-40 very insensitive
49
3 POSSIBLE DOSE-RESPONSE CURVES
50
• Establishes casualty that the chemical has
induced
• Establishes the lowest dose where an induced
effect occurs (the threshold effect)
• Determines the rate at which an injury builds up
DOSE-RESPONSE RELATIONSHIP
Typical shape –
small doses
have minimal
effect, then
increases
rapidly after
threshold
51
MEASURING TOXICITY
• ANIMAL TESTING
 Most commonly used and widely accepted
toxicity test is to expose a population of
laboratory animals to measured doses of
specific toxins.
• Humanitarian concerns in using animals
• Different individuals have different sensitivities
to the same toxin. Should we aim to protect the
average person or the most sensitive?
52
COMPLICATIONS IN MEASURING TOXICITY
• Unrelated species can react quite differently to
the same toxin due to differences in physiology
and metabolism.
- Dose Response Curves not symmetrical
 LD50 - DOSE AT WHICH 50% OF THE
ANIMAL TEST POPULATION DIES
• These variations make it difficult to estimate
the risk to humans.
53
• LD-50 is the measure used to indicate the
“lethal dose” of a material that, when given at
once, kills 50% of a group of test animals, such
as laboratory rats.
• For most animals, a safe concentration is
obtained by taking the LD-50 value and dividing
it by 10. The logic is that is the LD-50 value
causes 50% of the animals to die, then 10% of
the LD-50 value should cause few or no animals
to die.
• FOR HUMANS LD-50 and ED-50 values obtained
from rats and mice are divided by 1,000 to set
safe values
LD-50 Math Problems!!!
54
Problem:
Assume that for a certain pesticide, the LD-50
dosage level for laboratory rats is determined to
be 200 mg/kg of body mass.
1. Calculate the amount of the pesticide that
would be considered safe for animals to ingest?
2. Calculate what amount of pesticide would be
considered safe for humans to ingest?
LD-50 Math Problems!!!
55
TOXICITY RATINGS
 MODERATE TOXIN takes about 1g/kg of
body weight to produce a lethal dose.
 VERY TOXIC materials require about 10% of
that amount.
 EXTREMELY TOXIC materials require 1% of
that amount.
 SUPER TOXIC chemicals can be lethal in a
dose of a few micrograms (an amount
invisible to the naked eye).
56
ACUTE vs CHRONIC DOSES & EFFECTS
• ACUTE EFFECTS - caused by a single exposure
and results in an immediate health problem
• CHRONIC EFFECTS - Long-lasting, perhaps
permanent. Can be result of single large dose
or repeated smaller doses.
 Also refer to long-lasting exposures as
chronic
 Difficult to study the effects of chronic
exposure since aging or other diseases may
be acting as well.
57
RISK ASSESSMENT AND ACCEPTANCE
• RISK - possibility of suffering harm or loss
• RISK ASSESSMENT - scientific process of
estimating the threat that particular hazards
pose to human health
 Risk Identification
 Dose Response Assessment
 Exposure Appraisal
 Risk Characterization
58
RISK ANALYSIS – 3 STEPS
• STEP 1 – RISK ASSESSMENT
 QUALITATIVE is making a judgment based on a
perception
 Highway is wet, so we slow down
59
• STEP 1 – RISK ASSESSMENT cont...
 QUANTITATIVE
 Risk = probability of being exposed to a hazard
X probability of being harmed if exposed
 4 steps – identify hazard, dose-response
assessment, exposure assessment, risk
characterization
• STEP 2 – RISK ACCEPTANCE
 Determining the level or risk that is tolerated
 Tough to determine because different people
are willing to live with different amounts of risk
• STEP 3 – RISK MANAGEMENT
 Determines policy, considering economic,
social, political, and ethical practices
60
RISK ASSESSMENT IS NOT RATIONAL
• Interested parties tend to downplay or
emphasize risks to suit their agenda.
• We tend to tolerate risks we choose, while
objecting to risks that we cannot control.
• Most people do not understand probability.
• Personal experience can be misleading.
• We have an exaggerated view of our own
abilities. Most people consider themselves
above average drivers.
• News media over-report sensational events and
under-report mundane events, skewing our
perception of their frequency.
• Irrational fears
61
RISK ACCEPTANCE
• People will tolerate a high probability of an
occurrence if the harm caused is low.
• Great harm is acceptable only at very low levels
of frequency.
• For most people, a 1 in 100,000 chance of dying
is a threshold for changing behavior.
• Environmental Protection Agency assumes that
a risk of 1 in 1 million is acceptable for
environmental hazards.
 Risk of dying of lung cancer if you smoke is
1 in 4, while risk of drinking water
contaminated with the limit of
trichloroethylene is 1 in 10 million. Yet many
people are focused on the latter.
62
LIFETIME
CHANCES OF
DYING IN THE U.S.
63
THRESHOLDS
• The DELANEY CLAUSE (1958) of the U.S. Food
and Drug Act forbids the addition of any
amount of a known carcinogen into food and
drugs.
• This standard was impossible to meet and was
replaced in 1996 by a “no reasonable harm”
requirement defined as less than one cancer for
every million people exposed over a lifetime.
64
STOCKHOLM CONVENTION
 In 2001, a group of 127 nations gathered in
Stockholm, Sweden, to reach an agreement on
restricting the global use of some chemicals
 12 chemicals were to be banned, phased out, or
reduced
 All 12 are POP’s – Persistent Organic Pollutants
• PESTICIDES: aldrin, chlordane, DDT, dieldrin, endrin,
heptachlor, hexachlorobenzene, mirex, toxaphene;
• INDUSTRIAL CHEMICALS: hexachlorobenzene,
polychlorinated biphenyls (PCBs);
• BY-PRODUCTS: polychlorinated dibenzo-p-dioxins and
polychlorinated dibenzofurans (PCDD/PCDF)
65
ESTABLISHING HEALTH POLICY
• It is difficult to separate the effects of multiple
hazards and evaluate their risks accurately,
especially when exposures are near the
threshold of measurement and response.
• In setting standards, should consider:
 combined effects of exposure
 different sensitivities
 effects of chronic as well as acute exposure
• Not reasonable to be protected from every
contaminant no matter how small the risk
• We must consider the effects on other
organisms that maintain our environment.

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  • 2. 2 OUTLINE • ENVIRONMENTAL HEALTH  INFECTIOUS AND EMERGENT DISEASES  ANTIBIOTICS AND PESTICIDE RESISTANCE • TOXICOLOGY • MOVEMENT, DISTRIBUTION, AND FATE OF TOXINS • MINIMIZING TOXIC EFFECTS • MEASURING TOXICITY • RISK ASSESSMENT • ESTABLISHING HEALTH POLICY
  • 3. 3 ENVIRONMENTAL HEALTH • HEALTH - a state of complete physical, mental, and social well-being • DISEASE - an abnormal change in the body’s condition that impairs physical or psychological function, disrupting HOMEOSTASIS  Diet and nutrition, infectious agents, toxic chemicals, genetics, trauma and psychological stress all play roles in MORBIDITY (illness) and MORTALITY (death).
  • 5. 5 ENVIRONMENTAL HEALTH RISKS • PATHOGENS - INFECTIOUS AGENTS – bacteria, fungus, virus, parasite, protozoa, etc • TRAUMA – accidents • POLLUTION – air, water, noise, etc • RADIATION – UV, nuclear waste • TOXINS – smoking, metals like mercury & lead, chemical exposure from pesticides, herbicides, cleaning solution, etc.
  • 6. 6 Categories of Human Health Risk • The categories of health risk:  PHYSICAL – cause injury or loss of life (natural disaster, UV radiation, rock thrown at your head)  BIOLOGICAL – involved diseases (causes most deaths)  CHEMICAL – exposure to natural or synthetic chemicals (pesticides, pharmaceuticals, heavy metals)
  • 7. 7 Categories of Human Health Risk • Types of diseases  INFECTIOUS DISEASES are caused by pathogens, which include viruses, bacteria, fungi, protests, worms (transmitted by contact…COMMUNICABLE)  CHRONIC DISEASES slowly impair the functioning of a body (long lasting and recurrent) (heart disease, cancer)  ACUTE DISEASES rapidly impair bodily functions (flu, stroke) • Chronic much higher in developing countries due to poor sanitation, unsafe water, malnutrition, etc
  • 8. 8 GLOBAL DISEASE BURDEN • Life expectancy is increasing as infant mortality decreases. • Disability-adjusted life years (DALYs) – a tool that measures the effects of a disease on the population. DALY’s takes into account ALL effects of a disease. Not just the number of people who die from it. • Chronic conditions account for 60% of premature deaths and 50% of diseases and are becoming more prevalent.  By 2020, heart disease may become leading source of disability and disease worldwide. Global cancer rates will increase by 50%.
  • 9. 9 GLOBAL DISEASE BURDEN • DIABETES is on the increase. One-third of children born in North America today will develop diabetes in their lifetime due to poor diet and little exercise. • WHO projects that PSYCHOLOGICAL CONDITIONS could increase their share of the global disease burden from 10% currently to 15%.  DEPRESSION will be the second largest cause of all years lived with disability. • TOBACCO RELATED LUNG DISEASES are increasing. Biggest single cause of death worldwide.
  • 11. 11 COMMON VECTORS & DISEASES • VECTOR – the mode of transport for a pathogenic organism • INSECTS:  MOSQUITOES (malaria, dengue, yellow fever)  FLIES (sleeping sickness, typhoid, cholera)  TICKS (Lyme, Rocky Mt Spotted Fever) • WATER BORNE DISEASES: diarrheas, Hepatitis A, typhoid, cholera • VIRUSES: Hepatitis, HIV, measles, small pox • PROTOZOANS: malaria, giardia, trypanosomiasis • WORMS: tapeworm, flukes, schistosomiasis, elephantatiasis • RODENTS, BIRDS, etc. can also carry pathogens
  • 12. 12 INFECTIOUS DISEASES KILL PEOPLE • When a pathogen causes a rapid increase in disease, we call it an EPIDEMIC • When it occurs over a large geographic area, we call it a PANDEMIC • Transferred through spit/sneezing, contaminated foods/objects, vectors • Antibiotics are over prescribed and pathogens becoming resistant making “stronger” bacteria
  • 13. 13 INFECTIOUS DISEASES • Communicable diseases are still responsible for about 1/3 of all disease-related deaths. - Majority in countries with poor nutrition, sanitation, and vaccination  Malaria is a major disease in tropical areas. Two million people die each year. • Better nutrition, clean water, improved sanitation and inoculation of children could eliminate most of the deaths.
  • 14. 14 HISTORICAL DISEASES • PLAGUE caused by bacteria carried by fleas • MALARIA is caused by protists found in mosquitoes • TUBERCULOSIS is a highly contagious disease caused by bacteria that attacks the lungs • FLU - Greatest loss of life in a single year from a pathogen was in 1918 when the flu epidemic killed 50 to 100 million people worldwide. Today we are concerned that bird flu might cause an even larger outbreak.
  • 15. 15 EMERGENT DISEASES • An EMERGENT DISEASE is one never known before, or one which has been absent for at least 20 years. • Growing human populations push into remote areas where they encounter pathogens. • Air travel makes it possible to spread emergent diseases around the globe quickly.  West Nile virus (spread by mosquitoes) was introduced into North America in 1999, and is now found everywhere in the lower 48 states.
  • 16. 16 EMERGENT INFECTIOUS DISEASES • HIV - HUMAN IMMUNODEFICIENCY SYNDROME / Acquired Immune Deficiency Syndrome (AIDS) – came from chimps. Weakens immune system • EBOLA comes from primates. Fever, internal bleeding. No pandemic, but death within two weeks • MAD COW DISEASE – pathogen that damages cow’s nervous system. Can have same affect on humans (attack brain) • BIRD FLU – Small number infects now, but future worse • WEST NILE spread by mosquitoes • SARS (severe acute respiratory syndrome)
  • 18. 18 CONSERVATION MEDICINE • ECOLOGICAL DISEASES - ANIMAL EPIDEMICS  A viral hemorrhagic disease is killing fish in the Great Lakes; introduced through ballast.  California sea lions have herpes 1 virus spread to them from human sewage.  Mad Cow and Deer wasting Disease are spread by prions from animal to animal  Sudden oak death syndrome is killing oak, redwoods, Douglas fir trees. Fungus imported on nursery stock.
  • 19. 19 CONSERVATION MEDICINE • CONSERVATION MEDICINE - attempts to understand how environmental changes threaten the health of humans and natural communities • ZOONOTIC ILLNESS – diseases normally found in animals that can be spread to humans (Anthrax, Rabies, Lyme, Plague, West Nile, Tuberculosis, Brucellosis)
  • 20. 20 ANTIBIOTIC AND PESTICIDE RESISTANCE • WHAT CAUSES RESISTANCE?  Natural selection and the ability of organisms to evolve rapidly  Human tendency to overuse pesticides and antibiotics • IE: Protozoan parasite that causes malaria is now resistant to most antibiotics, while the mosquitoes that transmit it have developed resistance to many insecticides. And, Global Warming is widening the range of these insects.
  • 21. 21 ANTIBIOTIC USE • At least half of the 100 million antibiotic doses prescribed in the U.S. every year are unnecessary or are the wrong drug. • Many people do not finish the full-course. Allowing resistant bacteria to multiply. • More than half of all antibiotics manufactured in the U.S. are routinely fed to farm animals to stimulate weight gain. Excreted in urine and feces, they find their way into surface water.
  • 23. 23 FUNDING HEALTH CARE • Heaviest burden of illness borne by poorest people who cannot afford a healthy environment or adequate health care.  WHO estimates 90% of all disease burden occurs in developing countries where less than 10% of all health care dollars are spent. • Raising our investment in health care would boost the world economy, reduce the spread of pathogens, and reduce population growth since parents whose children survive have fewer offspring.
  • 24. 24
  • 25. 25 TOXICOLOGY • TOXICOLOGY is the study of poisons and their effects on living systems. • Dangerous chemicals are divided into two broad categories:  TOXIC - poisonous - Can be general or very specific. Often harmful even in dilute concentrations.  HAZARDOUS - dangerous - Flammable, explosive, irritant, acid, caustic • ECOTOXICOLOGY deals with the interactions, transformation, fate, and effects of natural and synthetic chemicals in the biosphere.
  • 26. 26 REMEMBER: The level of harmfulness depends on dose, frequency, genetic make up of those exposed, and health of those exposed TOXICOLOGY CHEMICALS OF CONCERN 7 CATEGORIES 1. IMMUNE SYSTEM DEPRESSANTS - pollutants that depress the immune system 2. ENDOCRINE DISRUPTERS - disrupt normal hormone functions (DDT, plastics)  cause low sperm count, breast cancer  Environmental estrogens - environmental contaminants which cause reproductive problems in animals even at very low doses
  • 27. 27 3. NEUROTOXINS - metabolic poisons that specifically attack nerve cells, cause organ failure (insecticides, lead, mercury). Different types act in different ways.  HEAVY METALS kill nerve cells.  ANESTHETICS AND CHLORINATED HYDROCARBONS disrupt nerve cell membranes.  ORGANOPHOSPHATES AND CARBAMATES inhibit signal transmission between nerve cells.
  • 28. 28 4. MUTAGENS - Agents that damage or alter genetic material. Can lead to birth defects or tumors. (chloroform, ethylene oxide, benzene, lead, and vinyl chloride) 5. TERATOGENS - specifically cause abnormalities during embryonic growth and development (nicotine, alcohol, drugs)  Alcohol - Fetal Alcohol Syndrome 6. CARCINOGENS - chemicals that cause cancer. Cause cell damage and causes bad cells to grow. Damage genetic material (radon, arsenic, PCB’s, asbestos)
  • 29. 29 ABNORMAL CELL GROWTH aka Tumors • Many carcinogens, teratogens, and mutagens are dangerous at levels far below their direct toxic effect because abnormal cell growth exerts a form of biological amplification. One cell mutated by a toxin can form a tumor that can potentially kill an individual. Remember... cells grow exponentially! BENIGN – a tumor that grows slowly and doesn’t interfere with normal cell functions MALIGNANT - a growth that grows rapidly and interferes with normal cell functions
  • 30. 30 7. ALLERGENS - substances that causes high response from immune system (mold, pollen, dander, peanuts)  ANTIGENS - substances that are recognized as foreign by white blood cells and stimulate the production of specific antibodies - Other allergens act indirectly by binding to other materials so they become antigenic.  SICK BUILDING SYNDROME (SBS) is a phenomenon affecting building occupants who claim to experience acute health and comfort effects that appear to be linked to time spent in a building, but where no specific illness or cause can be identified.
  • 33. 33 MOVEMENT, DISTRIBUTION, AND FATE OF TOXINS • SOLUBILITY - one of most important characteristics in determining the movement and storage of a toxin • Chemicals are divided into two major groups:  WATER SOLUBLE (dissolve in water) compounds move rapidly through the environment and have access to cells.  FAT SOLUBLE (dissolve in oil) compounds need a carrier to move through the environment, but once inside the body they penetrate tissues easily. They are stored in body fat and persist for many years.
  • 34. 34 EXPOSURE AND SUSCEPTIBILITY • Airborne toxins generally cause more ill health than any other exposure.  Lining of lungs easily absorbs toxins. • Food, water and skin contact are other ways to be exposed to toxins. • Largest toxin exposure reported in industrial settings • Condition of organism and timing of exposure also have strong influences on toxicity. Children more vulnerable than adults. • BODY BURDEN - accumulated toxins in the body
  • 35. 35 • BIOACCUMULATION selective absorption & storage of toxins  Dilute toxins in the environment can build to dangerous levels inside tissues. • BIOMAGNIFICATION Toxic burden of a large number of organisms at a lower trophic level is accumulated and concentrated by a predator at a higher trophic level.
  • 36. 36 PERSISTENCE • Some chemical compounds are very unstable and degrade rapidly under most conditions, thus their concentrations decline quickly after release. • Others are more persistent.  Stability can cause problems as toxins may be stored for a long period of time and spread to unintended victims PERSISTENCE- how long a chemical remains in the environment
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  • 38. 38 PERSISTENT ORGANIC POLLUTANTS - POP’s • FLAME RETARDANTS (PBDE) are now found in humans and other species everywhere in the world. Harm children’s reproductive and nervous systems. • NON-STICK PLASTIC COATINGS (PFOS and PFOA) are infinitely persistent in the environment and can be found in your blood. Cause liver damage and cancer. • PHTHALATES - found in plastics mimic estrogen and are linked to reproductive abnormalities and reduced fertility.
  • 39. 39 CHEMICAL INTERACTIONS • ANTAGONISTIC REACTION - one material interferes with the effects, or stimulates the breakdown, of other chemicals • ADDITIVE REACTION - effects of each chemical are added to one another • SYNERGISTIC REACTION - one substance exacerbates the effect of the other  Example: Asbestos exposure increases risk of lung cancer 20X; smoking has same risk. But together, they increase risk 400X.
  • 40. 40 MECHANISMS FOR MINIMIZING TOXIC EFFECTS • EVERY MATERIAL CAN BE POISONOUS UNDER CERTAIN CONDITIONS.  Most chemicals have a safe threshold under which their effects are insignificant. • METABOLIC DEGRADATION  In mammals, the LIVER is the primary site of detoxification of both natural and introduced poisons. - Sometimes compounds that are harmless can be broken down into products that are harmful.
  • 41. 41 EXCRETION AND REPAIR • Effects of waste products and environmental toxins reduced by eliminating via excretion.  Breathing  Urine • Tissues and organs often have mechanisms for damage repair by cellular reproduction.  Any irritating agent can be potentially carcinogenic because the more times that cells divide, the greater the chance that they will have a mistake (mutation) while copying their DNA. This can lead to cancer.
  • 42. 42 DOSE-RESPONSE STUDIES • EPIDEMIOLOGY - gathers data from large exposed populations over long periods and compares with a population group not exposed the threat • DOSE-RESPONSE ANALYSIS measures response of test animals to various doses of suspected toxicant  DOSE = the amount of toxicant the test animal receives  RESPONSE = the type or magnitude of negative effects of the animal  DOSE-RESPONSE CURVE = the plot of dose given against response
  • 43. 43 DOSE-RESPONSE STUDIES • LD50- “median Lethal Dose” that kills 50% of the individuals in 2 weeks • ED50- “median Effective Dose” that causes 50% of the animals to display the harmful but nonlethal effect • LC50 – “median Lethal Concentration” that kills 50% of aquatic species • Not very accurate as different animals & people respond differently. • Helps us determine at what levels of pollution, drugs, and other substances we should/should not be exposed.
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  • 47. 47 Most members in this population are similar, however there are extremes at both ends
  • 48. 48 0-10 very sensitive 10-30 relatively sensitive (20 is average) 30-40 very insensitive
  • 50. 50 • Establishes casualty that the chemical has induced • Establishes the lowest dose where an induced effect occurs (the threshold effect) • Determines the rate at which an injury builds up DOSE-RESPONSE RELATIONSHIP Typical shape – small doses have minimal effect, then increases rapidly after threshold
  • 51. 51 MEASURING TOXICITY • ANIMAL TESTING  Most commonly used and widely accepted toxicity test is to expose a population of laboratory animals to measured doses of specific toxins. • Humanitarian concerns in using animals • Different individuals have different sensitivities to the same toxin. Should we aim to protect the average person or the most sensitive?
  • 52. 52 COMPLICATIONS IN MEASURING TOXICITY • Unrelated species can react quite differently to the same toxin due to differences in physiology and metabolism. - Dose Response Curves not symmetrical  LD50 - DOSE AT WHICH 50% OF THE ANIMAL TEST POPULATION DIES • These variations make it difficult to estimate the risk to humans.
  • 53. 53 • LD-50 is the measure used to indicate the “lethal dose” of a material that, when given at once, kills 50% of a group of test animals, such as laboratory rats. • For most animals, a safe concentration is obtained by taking the LD-50 value and dividing it by 10. The logic is that is the LD-50 value causes 50% of the animals to die, then 10% of the LD-50 value should cause few or no animals to die. • FOR HUMANS LD-50 and ED-50 values obtained from rats and mice are divided by 1,000 to set safe values LD-50 Math Problems!!!
  • 54. 54 Problem: Assume that for a certain pesticide, the LD-50 dosage level for laboratory rats is determined to be 200 mg/kg of body mass. 1. Calculate the amount of the pesticide that would be considered safe for animals to ingest? 2. Calculate what amount of pesticide would be considered safe for humans to ingest? LD-50 Math Problems!!!
  • 55. 55 TOXICITY RATINGS  MODERATE TOXIN takes about 1g/kg of body weight to produce a lethal dose.  VERY TOXIC materials require about 10% of that amount.  EXTREMELY TOXIC materials require 1% of that amount.  SUPER TOXIC chemicals can be lethal in a dose of a few micrograms (an amount invisible to the naked eye).
  • 56. 56 ACUTE vs CHRONIC DOSES & EFFECTS • ACUTE EFFECTS - caused by a single exposure and results in an immediate health problem • CHRONIC EFFECTS - Long-lasting, perhaps permanent. Can be result of single large dose or repeated smaller doses.  Also refer to long-lasting exposures as chronic  Difficult to study the effects of chronic exposure since aging or other diseases may be acting as well.
  • 57. 57 RISK ASSESSMENT AND ACCEPTANCE • RISK - possibility of suffering harm or loss • RISK ASSESSMENT - scientific process of estimating the threat that particular hazards pose to human health  Risk Identification  Dose Response Assessment  Exposure Appraisal  Risk Characterization
  • 58. 58 RISK ANALYSIS – 3 STEPS • STEP 1 – RISK ASSESSMENT  QUALITATIVE is making a judgment based on a perception  Highway is wet, so we slow down
  • 59. 59 • STEP 1 – RISK ASSESSMENT cont...  QUANTITATIVE  Risk = probability of being exposed to a hazard X probability of being harmed if exposed  4 steps – identify hazard, dose-response assessment, exposure assessment, risk characterization • STEP 2 – RISK ACCEPTANCE  Determining the level or risk that is tolerated  Tough to determine because different people are willing to live with different amounts of risk • STEP 3 – RISK MANAGEMENT  Determines policy, considering economic, social, political, and ethical practices
  • 60. 60 RISK ASSESSMENT IS NOT RATIONAL • Interested parties tend to downplay or emphasize risks to suit their agenda. • We tend to tolerate risks we choose, while objecting to risks that we cannot control. • Most people do not understand probability. • Personal experience can be misleading. • We have an exaggerated view of our own abilities. Most people consider themselves above average drivers. • News media over-report sensational events and under-report mundane events, skewing our perception of their frequency. • Irrational fears
  • 61. 61 RISK ACCEPTANCE • People will tolerate a high probability of an occurrence if the harm caused is low. • Great harm is acceptable only at very low levels of frequency. • For most people, a 1 in 100,000 chance of dying is a threshold for changing behavior. • Environmental Protection Agency assumes that a risk of 1 in 1 million is acceptable for environmental hazards.  Risk of dying of lung cancer if you smoke is 1 in 4, while risk of drinking water contaminated with the limit of trichloroethylene is 1 in 10 million. Yet many people are focused on the latter.
  • 63. 63 THRESHOLDS • The DELANEY CLAUSE (1958) of the U.S. Food and Drug Act forbids the addition of any amount of a known carcinogen into food and drugs. • This standard was impossible to meet and was replaced in 1996 by a “no reasonable harm” requirement defined as less than one cancer for every million people exposed over a lifetime.
  • 64. 64 STOCKHOLM CONVENTION  In 2001, a group of 127 nations gathered in Stockholm, Sweden, to reach an agreement on restricting the global use of some chemicals  12 chemicals were to be banned, phased out, or reduced  All 12 are POP’s – Persistent Organic Pollutants • PESTICIDES: aldrin, chlordane, DDT, dieldrin, endrin, heptachlor, hexachlorobenzene, mirex, toxaphene; • INDUSTRIAL CHEMICALS: hexachlorobenzene, polychlorinated biphenyls (PCBs); • BY-PRODUCTS: polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/PCDF)
  • 65. 65 ESTABLISHING HEALTH POLICY • It is difficult to separate the effects of multiple hazards and evaluate their risks accurately, especially when exposures are near the threshold of measurement and response. • In setting standards, should consider:  combined effects of exposure  different sensitivities  effects of chronic as well as acute exposure • Not reasonable to be protected from every contaminant no matter how small the risk • We must consider the effects on other organisms that maintain our environment.